PIPA5100008

BBS2 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5100008-Each-of-1 In Stock ₹ 46,502.50

PIPA5100008 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

BBS2

Classification

Polyclonal

Conjugate

Unconjugated

Gene

BBS2

Gene Alias

2410125H22Rik; AI447581; Bardet-Biedl syndrome 2; Bardet-Biedl syndrome 2 (human); Bardet-Biedl syndrome 2 homolog; Bardet-Biedl syndrome 2 protein; Bardet-Biedl syndrome 2 protein homolog; BBS; bbs2; bbs2 protein; fb80a05; MGC20703; RP74; Unknown (protein for MGC:134372); wu:fb80a05

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

113948, 583, 67378

Content And Storage

-20°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide; pH 7.4

Gene Accession No.

Q99MH9, Q9BXC9, Q9CWF6

Gene Symbols

BBS2

Immunogen

A synthesized peptide derived from human BBS2(Accession Q9BXC9), corresponding to amino acid residues T639-K689.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

Related Products

Img

Thermo Scientific

PIPA5100128

--

Img

Thermo Scientific

PIPA5100220

--

Img

Thermo Scientific

PIPA5100247

--

Img

Thermo Scientific

PIPA5100177

--

Img

Thermo Scientific

PIPA5100191

--

Img

Thermo Scientific

PIPA5100068

--

Img

Thermo Scientific

PIPA5100141

--

Img

Thermo Scientific

PIPA5100093

--

Description

  • Antibody detects endogenous levels of total BBS2
  • This gene is a member of the Bardet-Biedl syndrome (BBS) gene family
  • Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and mental retardation
  • The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function
  • Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells
  • BBS proteins may also be involved in intracellular trafficking via microtubule-related transport
  • The protein encoded by this gene forms a multiprotein BBSome complex with six other BBS proteins.