Solarbio 알부민 함량 분석 키트 (Bromocresol 녹색 비색법)

제품개요

사양	세부
유효기간	6 개월
저장	2-8℃
단위	상자
영어 이름	Albumin Content Assay Kit (Bromocresol 녹색 비색법)
탐지 방법	분광 광도계/마이크로 플레이트 리더
사양	100T/96S

Product Components

시약 이름	사양	저장 조건
추출 용액	액체 110 밀리리터×1병	2-8℃
시약 1	액체 0.28 mL×1 vial	2-8℃
시약 2	액체 25 밀리리터×1병	2-8℃
시약 3	액체 0.3 mL×1 vial	2-8℃
표준 솔루션	액체 1 mL×1 vial	-20℃

솔루션 준비:

1. Color Development Solution:
   • Prepare the color development solution according to the number of samples by mixing Reagent One, 시약 2, and Reagent Three in the ratio of 10μL: 990μL: 10μL (1010μL for 5 tests). Mix thoroughly and use immediately.
2. 표준 솔루션:
   • 준비하다 10 mg/mL albumin standard solution. 사용하기 전에, take 200μL of the 10 mg/mL albumin standard solution and add 200μL of the extraction solution to prepare a 5 mg/mL albumin standard solution. Mix thoroughly and use immediately.

제품 설명:

• Albumin:
  • The liver synthesizes the main protein in human plasma.
  • An important nutrient that maintains plasma osmotic pressure.
  • Binds with various nutrients, 호르몬, and drugs.
  • Reflects the nutritional status of the body.
  • Used to screen for diseases affecting liver metabolic function (예를 들어, cirrhosis, liver damage, malnutrition, malignant tumors).
• 탐지 방법:
  • In a pH 4.2 buffer solution, serum albumin carries a positive charge.
  • In the presence of a non-ionic surfactant, albumin binds with the negatively charged dye Bromocresol Green.
  • Forms a blue-green complex.
  • The complex has an absorption peak at a wavelength of 630 nm.
  • Color intensity is directly proportional to the concentration of albumin.
• Reaction:
  • Albumin + Bromocresol Green → Blue-Green Complex (630 nm)

메모:

• Before the experiment, selecting 2-3 samples with expected large differences is recommended to conduct a preliminary experiment.
• 시료의 흡광도가 측정범위를 벗어나는 경우, diluting or increasing the sample volume is recommended for detection.

필수 장비 및 소모품 (to be prepared):

• Visible spectrophotometer/microplate reader
• 저온 원심분리기
• 분석 균형
• Microglass cuvettes/96-well plates
• Adjustable pipettes
• Mortar/homogenizer/ultrasonic cell disruptor
• 얼음과 증류수

절차:

샘플 처리 (The sample volume can be adjusted accordingly; specific ratios can be referenced from literature):

1. 조직 샘플:
   • Add extraction solution in a ratio of sample mass (g) 추출 용액 부피에 (밀리리터) ~의 1:5~10 (recommend weighing 0.1g of the sample and adding 1.0mL of extraction solution).
   • Homogenize the sample in an ice bath, then centrifuge at 4℃, 8000g에 대한 10 분.
   • Discard the pellet and keep the supernatant on ice for testing.
2. Bacterial/Cell Samples:
   • Add extraction solution in a ratio of bacterial/cell count (10^6) 추출 용액 부피에 (밀리리터) of 5~10:1 (recommend adding 1.0mL of extraction solution to 5 million bacteria/cells).
   • Disrupt the bacteria/cells in an ice bath using an ultrasonic cell disruptor (power 200W, ultrasonicate for 3s, 간격 7초, 총 시간 5 분).
   • 4℃에서 원심분리기, 8000g에 대한 10 분.
   • Discard the pellet and keep the supernatant on ice for testing.
3. Liquid Samples:
   • Measure directly.
   • If the liquid is turbid, centrifuge and use the supernatant for measurement.

1. Preparation of Visible Spectrophotometer/Microplate Reader:
   • Preheat the visible spectrophotometer/microplate reader for at least 30 분.
   • Set the wavelength to 630 nm.
   • Zero the visible spectrophotometer with distilled water.
2. Operation Table (Add the following reagents to micro glass cuvettes/96-well plates):

시약 이름 (μL)	시험관	표준 튜브	빈 튜브
견본	20	–	–
표준 솔루션	–	20	–
추출 용액	–	–	20
Color Development Solution	200	200	200

• Mix well and let stand at room temperature for 20 초.
• Measure the absorbance of each tube at 630 nm, recording the values as A_test, A_standard, and A_blank.
• Calculate ΔA_test = A_test – A_blank, and ΔA_standard = A_standard – A_blank.
• Note that the blank tube and standard tube only need to be measured 1-2 타임스.

메모: The length of the standing time can affect the detection results. It is recommended to react directly in the micro glass cuvettes/96-well plates for 20 seconds and then measure the absorbance.

Albumin Content Calculation

1. Calculation by Sample Protein Concentration

Albumin content (mg/mg 프로트) = ΔA measured × (C standard ÷ ΔA standard) × V sample ÷ (V sample × Cpr) = 5 × ΔA measured ÷ ΔA standard ÷ Cpr

2. Calculation by Sample Mass

Albumin content (mg/g 질량) = ΔA measured × (C standard ÷ ΔA standard) × V sample ÷ (W × V sample ÷ V sample total) = 5 × ΔA measured ÷ ΔA standard ÷ W

3. Calculation by Bacterial/Cell Number

Albumin content (mg/10^6 cells) = ΔA measured × (C standard ÷ ΔA standard) × V sample ÷ (V sample × N ÷ V sample total) = 5 × ΔA measured ÷ ΔA standard ÷ N

4. Calculation by Liquid Volume

Albumin content (mg/mL) = ΔA measured × (C standard ÷ ΔA standard) × V sample ÷ V sample = 5 × ΔA measured ÷ ΔA standard

Definitions:

• C standard: Standard tube concentration, 5 mg/mL;
• V sample: 샘플량 추가됨, 0.02밀리리터;
• V sample total: Total extract volume added, 1밀리리터;
• 심폐소생술: 샘플 단백질 농도, mg/mL;
• 여: Sample mass, g;
• N: Total number of bacteria/cells, in 10^6

노트:

1. If ΔA_test is less than 0.010 or the absorbance of the test tube is close to that of the blank tube, you can increase the sample volume before measurement. If ΔA_test is greater than 0.5, it is recommended to appropriately dilute the sample supernatant with extraction solution before measurement. Note to simultaneously adjust the calculation formula.
2. If the sample becomes turbid after adding the color developer, it is recommended to appropriately dilute the sample supernatant with extraction solution before measurement. Note to simultaneously adjust the calculation formula.

실험예:

1. Take 20μL of human serum sample, dilute it 10 times with extraction solution, follow the measurement steps, and measure it using a 96-well plate. 계산: ΔA_test = A_test – A_blank = 0.426 – 0.124 = 0.302, ΔA_standard = A_standard – A_blank = 0.406 – 0.124 = 0.282. Calculated based on liquid volume: Albumin Content (mg/mL) = 5 × ΔA_test ÷ ΔA_standard × 10 (dilution factor) = 53.546 mg/mL.